Chitosan/anionic surfactant microparticles synthesized by high pressure spraying method for removal of phenolic pollutants

Biopolymeric microparticles were prepared by rapid expansion of high pressure CO₂-chitosan (Chi) solution in sodium bis-(2-ethyl hexyl) sulfosuccinate (AOT) solution. At pressures higher than 2 MPa, ultrafine particles were formed while under this value, wires were obtained. The formation of Chi/AOT complex was confirmed by Fourier Transform Infrared (FTIR) Spectroscopy, whereas scanning electron microscopy was used to characterize the morphology, size and shape of the particles. The FTIR spectrum proved the interaction between the sulfonate groups of AOT and the amino groups of Chi. Microparticles are quasi-spherical in wet conditions and irregular after freeze drying, presenting a rough surface with many pores. Lyophilized hydrophobic microparticles were used to remove phenol and o-cresol from aqueous solution, and the adsorption process showed a maximum efficiency in the 7–8 pH range. The uptake of phenol and o-cresol increased with the amount of particles and decreased with increasing the pollutant concentration. The adsorption occurred rapidly in the first 60–120 minutes, and leveled off thereafter.      

Chip-nanoelectrospray quadrupole time-of-flight tandem mass spectrometry of meningioma gangliosides: a preliminary study

A strategy combining high-performance thin layer chromatography (HPTLC), laser densitometry, and fully automated chip-based nanoelectrospray (nanoESIchip) performed on a NanoMate robot coupled to QTOF-MS was developed, optimized, and for the first time applied for mapping and structural identification of gangliosides (GGs) extracted and purified from a human angioblastic meningioma specimen. While HPTLC pattern indicated only seven fractions migrating as GM3, GM2, GM1, GD3, GD1a (nLD1, LD1), GD1b, GT1b, and possibly GD2, due to the high sensitivity, mass accuracy, and ability to ionize minor species in complex mixtures, nanoESIchip-QTOF MS was able to discover significantly more GG species than ever reported in meningioma. Thirty-four distinct glycosphingolipid components of which five asialo, one GM4, nine GM3, two GM2, two GD3, nine GM1, and six GD1 differing in their ceramide compositions were identified. All structures presented long-chain bases with 18 carbon atoms, while the length of the fatty acid was found to vary from C11 to C25. MS screening results indicated also that the diversity of the expressed GM1 structures is higher than expected in view of the low proportions evidenced by densitometric quantification. Simultaneous fragmentation of meningioma-associated GM1 (d18:1/24:1) and GM1 (d18:1/24:0) by MS/MS using CID confirmed the postulated structures of the ceramide moieties and provided data on the glycan core, which document that for each of the GM1 (d18:1/24:1) and GM1 (d18:1/24:0) forms both GM1a and GM1b isomers are expressed in the investigated meningioma tissue.